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FDA 510(k)

MYSAFETY SYRINGE

K-Number: K111734 · 2011-09-06

ApplicantMedicalchain Intl. Corp.
Decision Date2011-09-06
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MYSAFETY SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Medicalchain Intl. Corp.. It received FDA 510(k) clearance on 2011-09-06 under 510(k) number K111734. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYSAFETY SYRINGE?

MYSAFETY SYRINGE is a medical device that received FDA 510(k) clearance on 2011-09-06. The listed applicant is Medicalchain Intl. Corp.. The 510(k) number is K111734.

When did MYSAFETY SYRINGE receive FDA 510(k) clearance?

MYSAFETY SYRINGE received FDA 510(k) clearance on 2011-09-06, under 510(k) number K111734.

Who is the listed applicant for MYSAFETY SYRINGE?

The FDA 510(k) record lists Medicalchain Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MYSAFETY SYRINGE?

The FDA product code for MYSAFETY SYRINGE is MEG.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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